摘要
We report here a rare case ofDPY19L2 gene deletion at chromosome 12 breakpoints caused by a 46, XY, t （4; 12）; （q27; qlS） balanced translocation. The patient eventually developed globozoospermia. A 32-year-old male had experienced infertility issues for 4 years.The patient exhibited normal appearance, intelligence, and body type, with a height of 175 cm and a weight of 75 kg.
We report here a rare case ofDPY19L2 gene deletion at chromosome 12 breakpoints caused by a 46, XY, t （4; 12）; （q27; qlS） balanced translocation. The patient eventually developed globozoospermia. A 32-year-old male had experienced infertility issues for 4 years.The patient exhibited normal appearance, intelligence, and body type, with a height of 175 cm and a weight of 75 kg.
